| Product NDC: | 52389-241 | 
| Proprietary Name: | Uricalm | 
| Non Proprietary Name: | Phenazopyridine Hydochloride | 
| Active Ingredient(s): | 99.5 mg/1 & nbsp; Phenazopyridine Hydochloride | 
| Administration Route(s): | ORAL | 
| Dosage Form(s): | TABLET, FILM COATED | 
| Coding System: | National Drug Codes(NDC) | 
| Product NDC: | 52389-241 | 
| Labeler Name: | Alva-Amco Pharmacal Companies, Inc. | 
| Product Type: | HUMAN OTC DRUG | 
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER | 
| Start Marketing Date: | 20080429 | 
| Package NDC: | 52389-241-12 | 
| Package Description: | 1 BLISTER PACK in 1 CARTON (52389-241-12) > 12 TABLET, FILM COATED in 1 BLISTER PACK (52389-241-02) | 
| NDC Code | 52389-241-12 | 
| Proprietary Name | Uricalm | 
| Package Description | 1 BLISTER PACK in 1 CARTON (52389-241-12) > 12 TABLET, FILM COATED in 1 BLISTER PACK (52389-241-02) | 
| Product NDC | 52389-241 | 
| Product Type Name | HUMAN OTC DRUG | 
| Non Proprietary Name | Phenazopyridine Hydochloride | 
| Dosage Form Name | TABLET, FILM COATED | 
| Route Name | ORAL | 
| Start Marketing Date | 20080429 | 
| Marketing Category Name | UNAPPROVED DRUG OTHER | 
| Labeler Name | Alva-Amco Pharmacal Companies, Inc. | 
| Substance Name | PHENAZOPYRIDINE HYDROCHLORIDE | 
| Strength Number | 99.5 | 
| Strength Unit | mg/1 | 
| Pharmaceutical Classes |